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MC 55 055 001 E - r8 - A950 - UG PDF
MC 55 055 001 E - r8 - A950 - UG PDF
©2013 Bovie Medical Corporation. All rights reserved. Contents of this publication may not be reproduced without
the written permission of Bovie Medical Corporation.
CAUTION:
Indicates a hazardous situation which, if not avoided, may result in minor or moderate injury.
NOTICE:
Indicates an operating tip, a maintenance suggestion, or a hazard that may result in product
damage.
l Key Features
l Safety
CAUTIONS
Read all warnings, cautions, and instructions provided with this generator before using.
Read the instructions, warnings, and cautions provided with electrosurgical accessories before using. Specific instruc-
tions are not included in this manual.
• Presets
The unit incorporates six user-defined presets for easy recall of frequently used settings.
• Self diagnostics
These diagnostics continually monitor the unit to ensure proper performance.
SAFETY
The safe and effective use of electrosurgery depends to a large degree on factors solely under the control of the
operator. There is no substitute for a properly trained and vigilant medical staff. It is important that they read,
understand, and follow the operating instructions supplied with this electrosurgical equipment.
Physicians have used electrosurgical equipment safely in numerous procedures. Before starting any surgical procedure,
the surgeon should be familiar with the medical literature, complications, and hazards of using electrosurgery in that
procedure.
To promote the safe use of the Aaron 950™ Electrosurgical Generator, this section presents the warnings and
cautions that appear throughout this user’s guide. So that you can operate this equipment with maximum safety,
it is important that you read, understand, and follow the instructions in these warnings and cautions. It is also
important that you read, understand, and follow the instructions for use in this user’s guide.
WARNINGS:
Hazardous Electrical Output - This equipment is for use only by trained, licensed physicians.
Danger: Fire / Explosion Hazard - Do not use the Aaron 950™ electrosurgical generator in the presence of
flammable anesthetics.
• Position the patient return electrode to provide a direct current route between the surgical
site and the return electrode which avoids skin-to-skin contact areas.
• In addition, place patient return electrodes according to the manufacturer’s instructions.
Potential for alternate site burns increases if the return electrode is compromised.
Do not wrap the accessory cords or patient return electrode cords around metal objects. This
may induce currents that could lead to shocks, fires, or injury to the patient or surgical team.
CAUTIONS:
At no time should you touch the active electrode or bipolar forceps. A burn could result.
Do not stack equipment on top of the generator or place the generator on top of electrical equipment. These
configurations are unstable and/or do not allow adequate cooling.
Provide as much distance as possible between the electrosurgical generator and other electronic equipment (such as
monitors). An activated electrosurgical generator may cause interference with them.
Nonfunction of the generator may cause interruption of surgery. A backup generator should be available for use.
Do not turn the activation tone down to an inaudible level. The activation tone alerts the surgical team when an
accessory is active.
When using a smoke evacuator in conjunction with the electrosurgical generator, place the smoke evacuator a
distance from the generator and set the generator volume control at a level that ensures that the activation tones
can be heard.
The use of high frequency current can interfere with the function of other electromagnetic equipment.
When high frequency surgical equipment and physiological monitoring equipment are used simultaneously on the
same patient, place any monitoring electrodes as far as possible from the surgical electrodes. Monitoring systems
incorporating high frequency current limiting devices are recommended.
Do not use needles as monitoring electrodes during electrosurgical procedures. Inadvertent electrosurgical burns may
result.
To avoid the possibility of an electrosurgical burn to either the patient or the physicians, do not allow the patient to
come in contact with a grounded metal object during activation. When activating the unit, do not allow direct skin
contact between the patient and the physician.
Remove any loose fitting jewelry from the patient before activation.
Examine all accessories and connections to the electrosurgical generator before use. Ensure that the accessories
function as intended. Improper connection may result in arcs, sparks, accessory malfunction, or unintended surgical
effects.
When not using active accessories, place them in a holster or in a clean, dry, nonconductive,
and highly visible area not in contact with the patient. Inadvertent contact with the patient may result in burns.
Studies have shown that smoke generated during electrosurgical procedures can be potentially harmful to patients
and the surgical team. These studies recommend adequately ventilating the smoke by using a surgical smoke
evacuator or other means.1
1. U.S. Department of Health and Human Services. National Institute for Occupational Safety
and Health (NIOSH). Control of Smoke from Laser / Electric Surgical Procedures. HAZARD
CONTROLS, Publication No. 96-128, September, 1996.
NOTICE:
Do not clean the generator with abrasive cleaning or disinfectant compounds, solvents, or other
materials that could scratch the panels or damage the generator.
SYMBOLS DESCRIPTION
Generator Controls
Cut mode
Blend mode
Coagulation mode
Bipolar mode
Fulguration mode
Presets
Indicators
RF ground referenced
Handpiece Connectors
Monopolar handpiece
Footswitch
Bipolar forceps
RF Isolated Indicator
Indicates when the
RF output is isolated from
the ground.
Power Output
Control Knob
Turn clockwise to increase
Coag Mode Selector Coag Indicator power output, counterclock-
When pressed, selects the Indicates when wise to decrease power
coagulation mode. coagulation mode is output.
selected.
RF Ground Referenced
Indicator
Indicates when the RF
output is ground refer-
enced. Only applies to Power Output
the fulguration mode. Control Knob
Turn clockwise to increase
power output, counterclock-
wise to decrease power
output.
Presets Display Presets Recall Selector Presets Set Button
Indicates which preset is selected (A- When pressed, selects the When depressed for 2 seconds,
F). “b” and “d” are displayed in lower- next preset setting. makes the current settings the
case letters. preset letter shown in the indi-
cator window.
No Presets Indicator
Dot blinks to indicate when
no user defined preset is
being used.
Monopolar Handpiece Patient Plate Grounding Bipolar Cord Receptacle Footswitch Receptacle
Receptacle Receptacle Accepts the Aaron A827EU bipolar Accepts the Aaron A1203W
Accepts the Aaron A901 Accepts the Aaron A1202C forceps cord. footswitch cord.
3-button handpiece cord. reusable grounding cord.
Volume control
Fuse enclosed
Manufacturer
NOTICE:
Please note that infected medical devices must be disposed of as medical/biohazard waste and cannot be includ-
ed in used electronic equipment disposal/recycling programs. In addition, certain electronic products must be
returned directly to Bovie Medical Corporation. Contact your Bovie® sales representative for return instructions.
SYMBOLS DESCRIPTION
Non-ionizing Radiation
● Initial Inspection
• Verify that the shipping package contains all items listed on the packing list.
If the unit or any accessories are damaged, notify Bovie Medical Corporation’s Customer Service immediately. Do not
use any damaged equipment.
CAUTION:
The unit is not to be utilized in the horizontal position, as liquids may easily spill into the unit.
If mounting on a wall surface, a qualified individual should be consulted to avoid damage to the
wall surface.
2. Plug the female end of the supplied power cord into the base of the unit and the male end into a grounded
wall receptacle.
WARNING:
Connect the power cord to a properly polarized and grounded power source with the frequency
and voltage characteristics that match those listed on the back of the unit.
l Setup Safety
l Setting Up
l Activation Safety
CAUTIONS
Read all warnings, cautions, and instructions provided with this generator before use.
Read the instructions, warnings, and cautions provided with electrosurgical accessories before use. Specific instruc-
tions are not included in this manual.
• Inspect for damage to the Electrosurgical Generator and all its connections.
• Inspect all cords and connectors for signs of wear, damage, and abrasion.
SETUP SAFETY
WARNINGS
Hazardous Electrical Output - This equipment is for use only by trained, licensed physicians.
Electric Shock Hazard - Connect the generator power cord to a properly grounded receptacle. Do not use power
plug adapters.
Connect the power cord to a properly polarized and grounded power source with the frequency and voltage charac-
teristics that match those listed on the back of the unit.
Fire Hazard - Do not use extension cords.
Patient Safety - Use the generator only if the self-test has been completed as described. Otherwise, inaccurate
power outputs may result.
The instrument receptacles on this generator are designed to accept only one instrument at a time. Do not attempt
to connect more than one instrument at a time into a given receptacle. Doing so will cause simultaneous activation
of the instruments.
Failure of the high frequency electrosurgical equipment could result in an unintended increase of output power.
Do not use electrosurgical equipment unless properly trained to use it in the specific procedure being undertaken.
Use by physicians without such training has resulted in serious, unintended patient injury, including bowel perfora-
tion and unintended, irreversible tissue necrosis.
For surgical procedures where the high frequency current could flow through parts of the body having a relatively
small cross-sectional area, the use of bipolar techniques may be desirable to avoid unwanted coagulation.
If the patient has an Implantable Cardioverter Defibrillator (ICD), contact the ICD manufacturer for instructions before
performing an electrosurgical procedure. Electrosurgery may cause multiple activation of ICDs.
In some circumstances, potential exists for alternate site burns at points of skin contact (e.g., between the arm and
the side of the body). This occurs when electrosurgical current seeks a path to the patient return electrode that
includes the skin-to-skin contact point. Current passing through small skin-to-skin contact points is concentrated and
may cause a burn. This is true for grounded, ground referenced, and isolated output generators.
To reduce the potential for alternate site burns, do one or more of the following:
• Avoid skin-to-skin contact points, such as fingers touching leg, when positioning the patient.
• Place 5 to 8 cm (2 to 3 in.) of dry gauze between contact points to ensure that contact does
not occur.
• Position the patient return electrode to provide a direct current route between the surgical
site and the return electrode which avoids skin-to-skin contact areas.
• In addition, place patient return electrodes according to the manufacturer’s instructions.
Potential for alternate site burns increases if the return electrode is compromised.
NOTICES
If required by local codes, connect the generator to the hospital equalization connector with an equipotential cable.
Connect the power cord to a wall outlet having the correct voltage. Otherwise product damage may result.
SETTING UP
1. If the unit is not already installed refer to Section 3 of this manual for the installation procedure.
2. Turn on the generator by pressing the power switch ON (|) (see figure 4-1, letter G). [Figure 4-1 is located at the end of this Section].
Verify the following:
• All visual indicators and displays on the front panel illuminate.
• Activation tones sound to verify that the speaker is working properly.
If the self-test is not successful, an alarm tone sounds. An error code may appear on the power display, in most
cases, the generator is disabled. Note the error code and refer to Section 6, Troubleshooting.
Once the self-test is successful, connect the accessories and set the generator controls. Refer to Preparing for
Monopolar Surgery or Preparing for Bipolar Surgery later in this section.
Select the desired mode to be stored by pressing one of the mode membrane switches (see figure 4-1, letter A)
Select the desired power to be stored by utilizing the power output control knob. (see figure 4-1, letter J).
Once all the settings are selected, depress and hold the Presets Set Button (see figure 4-1, letter I) for 2 seconds.
To indicate the settings have been stored, the letter on the Presets indicator will blink.
To recall a preset simply press the Presets Recall button to toggle through all the presets.
NOTICE:
A small dot blinking in the lower left corner of the Presets indicator indicates that the unit is not presently set to a user-
defined preset.
1. Plug the handpiece into the monopolar output on the lower left of the front of the unit (see figure 4-1, letter B).
The plug is designed to fit in only one direction. Plug the smaller round connector from the handpiece into the
receptacle on the bottom of the unit. The three button handpiece is designed to give the doctor complete fingertip
control of the power settings. The Aaron A901 handpiece is unique: handpieces manufactured by other manufac-
turers will not function with this unit. Do not use the Aaron A901 handpiece on other brand units.
2. Slide the desired active electrode into the handpiece until it is firmly seated (see figure 4-1, letter M). The handpiece will
accept most standard 3/32” (.24 cm) electrodes.
3. Slide the handpiece from above into the holder on the right side of the unit.
4. Plug the male end of the reusable grounding cord into the Patient Plate receptacle located to the right of the
monopolar output (see figure 4-1, letter C). Remove the disposable dispersive electrode from its pouch and attach to the
snap connector on the end of the reusable grounding cord.
NOTICE:
A return electrode is not required for the fulguration mode. The patient plate alarm is not used for this mode. Procedures
may be performed without the use of a return electrode.
5. An optional footswitch may be used with monopolar procedures. If the footswitch is utilized, plug the footswitch
cable into the footswitch jack (see figure 4-1, letter E). While using a footswitch the output will be delivered via the hand-
piece. The activation button on the handpiece will continue to function while a footswitch is connected to
the unit.
7. Set the output power either by using the dial on the front of the unit (see figure 4-1, letter J) or by the up and down but-
tons on the handpiece (see figure 4-1, letter K). When power level adjustment is being made by the handpiece an audible
tone will sound to indicate that the power level has been changed. Depressing and holding the up or down buttons
will cause the power settings to change more rapidly for quick adjustment of the output power. Power output is dis-
played in one watt increments for Cut, Blend, and Coagulation mode. The maximum power for each of these
modes is 60 watts. Power is displayed in “.1” watt increments below ten watts and in whole numbers from ten to 35
watts.
NOTICE:
The output settings cannot be adjusted when the unit is being activated.
8. The unit is now ready to perform surgery. Refer to Activating the Unit later in this section.
2. Connect the desired forcep to the operating end of the bipolar cord.
3. Plug the footswitch cable into the footswitch jack (see figure 4-1, letter E). A footswitch is required to activate the
Bipolar mode.
NOTICE:
Dispersive electrodes are not utilized during bipolar procedures.
4. Select the Bipolar mode by pressing the membrane switch on the front of the unit (see figure 4-1, letter A).
5. Set the output power either by using the dial on the front of the unit (see figure 4-1, letter J) or by the up and down but-
tons on the handpiece (see figure 4-1, letter K). When power level adjustment is being made by the handpiece an audible
tone will sound to indicate that the power level has been changed. Depressing and holding the up or down buttons
will cause the power settings to change more rapidly for quick adjustment of the output power. Power is displayed
in “.1” watt increments below ten watts and in whole numbers from ten to 30 watts.
NOTICE:
The output settings cannot be adjusted when the unit is being activated.
6. The unit is now ready to perform surgery. Refer to Activating the Unit later in this section.
CAUTIONS
The use of high frequency current can interfere with the function of other electromagnetic equipment.
When high frequency surgical equipment and physiological monitoring equipment are used simultaneously on the
same patient, place any monitoring electrodes as far as possible from the surgical electrodes. Monitoring systems
incorporating high frequency current limiting devices are recommended.
Do not use needles as monitoring electrodes during electrosurgical procedures. Inadvertent electrosurgical burns may
result.
To avoid the possibility of an electrosurgical burn to either the patient or the physicians, do not allow the patient to
come in contact with a grounded metal object during activation. When activating the unit, do not allow direct skin
contact between the patient and the physician.
Remove any loose fitting jewelry from the patient before activation.
Examine all accessories and connections to the electrosurgical generator before use. Ensure that the accessories func-
tion as intended. Improper connection may result in arcs, sparks, accessory malfunction, or unintended surgical
effects.
When not using active accessories, place them in a holster or in a clean, dry, nonconductive, and highly visible area
not in contact with the patient. Inadvertent contact with the patient may result in burns.
Studies have shown that smoke generated during electrosurgical procedures can be potentially harmful to patients
and the surgical team. These studies recommend adequately ventilating the smoke by using a surgical smoke evacua-
tor or other means.1
1. U.S. Department of Health and Human Services. National Institute for Occupational Safety and Health (NIOSH). Control
of Smoke from Laser / Electric Surgical Procedures. HAZARD CONTROLS, Publication No. 96-128, September, 1996.
2. Remove the handpiece from the holder. Place the handpiece in the desired position.
3. To activate the unit, depress the activation button on the handpiece (see figure 4-1, letter L) or depress the pedal on the
footswitch. While the unit is activated, the appropriate audible tone is sounded and one of the activation LEDs will
illuminate (see figure 4-1, letter N).
5. Return the handpiece to the holder on the right side of the unit and remove the electrode. The electrode should be
disposed of after each procedure. If contamination has occurred to the handpiece, the handpiece should be
sterilized.
NOTICE:
When sterilizing the handpiece follow the manufacturer’s sterilization instructions that accompany the handpiece.
Bipolar Activation
1. If the unit is not already set up, follow the set up procedure to prepare the unit for operation.
3. To activate the unit depress the footswitch pedal. While the unit is activated, an audible tone is sounded and the
blue activation LED will illuminate (see figure 4-1, letter N).
NOTICE:
When sterilizing the forceps follow the manufactures sterilization instructions that accompany the forceps.
l Cleaning
l Periodic Inspection
CLEANING
After each use, clean the unit.
WARNING:
Electric Shock Hazard - Always turn off and unplug the generator before cleaning.
NOTICE:
Do not clean the generator with abrasive cleaning or disinfectant compounds, solvents, or other
materials that could scratch the panels or damage the generator.
1. Turn off the generator, and unplug the power cord from the wall outlet.
2. Thoroughly wipe all surfaces of the generator and power cord with a mild cleaning solution or disinfectant and
a damp cloth. Follow the procedures approved by your institution or use a validated infection control procedure.
Do not allow fluids to enter the chassis. Do not sterilize the generator.
PERIODIC INSPECTION
Every six months, visually inspect the Aaron 950™ Electrosurgical Generator for signs of wear or damage.
In particular, look for any of the following problems:
Most error codes result from faults in accessories attached to the unit. The following table lists the error codes,
describes the error, and recommends actions to take to resolve the error.
1. Turn off, then turn on the generator. Do not press buttons or activate
accessory devices during the self-test.
2. If the error code reappears, disconnect all accessories.
Handswitch or monopolar Turn off, then turn on the generator again.
F1
footswitch pedal may be stuck 3. If the problem persists, replace the handpiece or footswitch
and repeat the restart.
4. If the error code reappears, record the number and call
Bovie Medical Corporation customer service.
• The user has followed the installation and setup procedures in this user’s guide.
• Persons authorized by Bovie Medical Corporation performed assembly operation, readjustments, modifications,
or repairs.
• The electrical installation of the relevant room complies with local codes and regulatory requirements, such as
IEC and BSI.
• Equipment use is in accordance with the Bovie Medical Corporation instructions for use.
NOTICE:
Do not clean the generator with abrasive cleaning or disinfectant compounds, solvents, or other
materials that could scratch the panels or damage the generator.
A. Turn off the generator, and unplug the power cord from the wall outlet.
B. Thoroughly wipe all surfaces of the generator and power cord with a mild cleaning solution or disinfectant and
a damp cloth. Follow the procedures approved by your institution or use a validated infection control procedure.
Do not allow fluids to enter the chassis. You cannot sterilize the generator.
B. Be sure the generator is completely dry before you pack it for shipment. Package it in its original shipping
container, if available.
C. Ship the generator, prepaid, to the address given to you by the Bovie Medical Corporation Service Center.
Duty Cycle
Under maximum power settings and rated load conditions (Pure Cut, 60 watt @ 500 Ω load), the generator is
suitable for activation times of 10 seconds on, 30 seconds off for one hour.
Operating Parameters
Ambient temperature range +10° to +40° C
Relative humidity 30% to 75%, non-condensing
Atmospheric pressure 70kPa to 106kPa
If transported or stored at temperatures outside the operating temperature range, allow one hour
Warm-up time
for the generator to reach room temperature before use.
Activation Tone
Volume (adjustable) 40 to 65 dB
Frequency Cut: 1 kHz
Blend: 1 kHz
Coagulation: 2 kHz
Fulguration: 2 kHz
Bipolar: 2 kHz
Duration Continuous while the generator is activated
Alarm Tone
Volume (not adjustable) 70 dB ± 5 dB
Frequency 2 kHz 1⁄2 seconds / 1 kHz 1⁄2 seconds
Duration 2s
Electromagnetic Interference
When other equipment is placed on or beneath an activated Bovie Medical Corporation electrosurgical generator, the
Aaron 950™ Electrosurgical Generator operates without interference. The generator minimizes electromagnetic inter-
ference to video equipment used in the operating room.
EMC COMPLIANCE
Special precautions should be taken regarding the Aaron 950™. Medical Electrical Equipment needs special precau-
tions regarding EMC and needs to be installed and put into service according to the EMC information provided in
this manual.
Understand that only the Accessories supplied with or ordered from Bovie® should be used with your device. The
use of accessories, transducers, and cables other than those specified, may result in increased Emissions or decreased
Immunity of the Aaron 950™. The Aaron 950™and its accessories are not suitable for interconnection with other
equipment.
Portable and mobile RF communications equipment can affect Medical Electrical Equipment. The Aaron 950™
should not be used adjacent to or stacked with other equipment and that if adjacent or stacked use is necessary, the
Aaron 950™ should be observed to verify normal operation in the configuration in which it will be used.
For transmitters rated at a maximum output power not listed above, the recommended separation
distance d in metres (m) can be estimated using the equation applicable to the frequency of the
transmitter, where P is the maximum output power rating of the transmitter in watts (W) according to
the transmitter manufacturer.
NOTE 1 At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is
affected by absorption and reflection from structures, objects and people.
The Aaron 950™ is intended for use in the electromagnetic environment listed below. The customer
or the user of the Aaron 950™ should assure that it is used in such an environment.
Emissions test Compliance Electromagnetic environment - guidance
The Aaron 950™ is intended for use in the electromagnetic environment listed below. The customer or
the user of the Aaron 950™ should assure that it is used in such an environment.
IEC 60601
Immunity test Compliance level Electromagnetic environment - guidance
test level
<5 % Ut <5 % Ut
(<95 % dip in Ut) (<95 % dip in Ut)
Mains power quality should be
for 0.5 cycle for 0.5 cycle
that of a typical commercial or
<40 % Ut <40 % Ut hospital environment. If the user
Voltage dips, short (<60 % dip in Ut) (<60 % dip in Ut) of the Aaron 950™ requires
interruptions and voltage for 5 cycles
for 5 cycles continued operation during power
variations on power sup-
70 % Ut 70 % Ut mains interruptions, it is
ply input lines
(<30 % dip in Ut) (<30 % dip in Ut) recommended that the Aaron
IEC 61000-4-11
for 25 cycles for 25 cycles 950™ be powered from an
uninterruptible power supply or a
<5 % Ut <5 % Ut
(>95 % dip in Ut) (>95 % dip in Ut) battery.
for 5 sec for 5 sec
Power frequency magnetic fields
Power frequency (50/60 should be at levels characteristic
Hz) magnetic field 3 A/m 3 A/m of a typical location in a typical
IEC 61000-4-8 commercial or hospital
environment.
NOTE Ut is the a.c. mains voltage prior to application of the test level.
d = [7 ]√ P
E1
800 MHz to 2.5 GHz
where P is the maximum output power rating
of the transmitter in watts (W) according to the
3 V/m transmitter manufacturer and d is the
Radiated RF recommended separation distance in metres
80 MHz to 3 V/m
IEC 61000-4-3 (m)
2.5 GHz
Field strengths from fixed RF transmitters, as
determined by an electromagnetic site survey,a
should be less than the compliance level in
each frequency range.b
Interference may occur in the vicinity of
equipment marked with the following
symbol.
NOTE 1 At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is
affected by absorption and reflection from structures, objects and people.
a Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones
and land mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be
predicated theoretically with accuracy. To assess the electromagnetic environment due to fixed RF
transmitters, an electromagnetic site survey should be considered. If the measured field strength in the
location which the Aaron 950™ is used exceeds the applicable RF compliance level above, the
Aaron 950™ should be observed to verify normal operation. If abnormal performance is observed,
additional measures may be necessary, such as reorienting or relocating the Aaron 950™.
b Over the frequency range 150 kHz to 80 MHz, field strengths should be less than [V1] V/m.
Bovie Medical Corporation’s obligation under this warranty is limited to the repair or replacement, at its sole option,
of any product, or part thereof, which has been returned to it or its Distributor within the applicable time period
shown below after delivery of the product to the original purchaser, and which examination discloses, to Bovie
Medical Corporation’s satisfaction, that the product is indeed, defective.
This warranty does not apply to any product, or part thereof, which has been repaired or altered outside Bovie
Medical Corporation’s factory in a way so as, in Bovie Medical Corporation’s judgment, to affect its stability or
reliability, or which has been subjected to misuse, neglect, or accident.
The warranty periods for Bovie Medical Corporation products are as follows:
Bovie Medical Corporation neither assumes nor authorizes any other person to assume for it any other liability in
connection with the sale or use of any of Bovie Medical Corporation’s products.
Notwithstanding any other provision herein or in any other document or communication, Bovie Medical
Corporation’s liability with respect to this agreement and products sold hereunder shall be limited to the aggregate
purchase price for the goods sold by Bovie Medical Corporation to the customer.
Bovie Medical Corporation disclaims any liability hereunder or elsewhere in connection with the sale of this product,
for indirect or consequential damages.
This warranty and the rights and obligations hereunder shall be construed under and governed by the laws of the
State of Florida, USA.
The sole forum for resolving disputes arising under or relating in any way to this warranty is the District Court of the
County of Pinellas, State of Florida, USA.
Bovie Medical Corporation, its dealers, and representatives reserve the right to make changes in equipment built
and/or sold by them at any time without incurring any obligation to make the same or similar changes on equipment
previously built and/or sold by them.